Keratinocyte growth factor protects mice from chemotherapy and radiation-induced gastrointestinal injury and mortality
- PMID: 9500453
Keratinocyte growth factor protects mice from chemotherapy and radiation-induced gastrointestinal injury and mortality
Abstract
Keratinocyte growth factor (KGF) stimulates the proliferation and differentiation of epithelial cells including those of the gastrointestinal tract. Although chemotherapeutics and radiation exposure kill rapidly proliferating tumor cells, rapidly dividing normal cells of the host's gastrointestinal tract are also frequently damaged, leading to the clinical condition broadly termed "mucositis." In this report, recombinant human KGF used as a pretreatment in several mouse models of chemotherapy and/or radiation-induced gastrointestinal injury significantly improved mouse survival. Using multiple-dose 5-fluorouracil, methotrexate, and radiation in combination and total body radiation alone models, KGF increased survival by 55% or greater. In the models that used chemotherapy with or without radiation, KGF significantly ameliorated weight loss after injury and accelerated weight gain during recovery. The basis of these systemic benefits appears to be due in part to the trophic effects of the growth factor on the intestinal epithelium because KGF pretreatment caused an increase in measures of mucosal thickness (villus height and crypt depth) that persisted during the course of 5-fluorouracil chemotherapy. Treatment with KGF also afforded a 3.5-fold improvement in crypt survival in the small intestine, suggesting that KGF also has a direct effect on the crypt stem cells. These data indicate that KGF may be therapeutically useful to lessen the intestinal side effects of current cancer therapy regimens.
Similar articles
-
Enhancement of murine intestinal stem cell survival after irradiation by keratinocyte growth factor.Radiat Res. 1997 Sep;148(3):248-53. Radiat Res. 1997. PMID: 9291356
-
The effect of keratinocyte growth factor on tumour growth and small intestinal mucositis after chemotherapy in the rat with breast cancer.Cancer Chemother Pharmacol. 2002 Jul;50(1):53-8. doi: 10.1007/s00280-002-0460-4. Epub 2002 May 14. Cancer Chemother Pharmacol. 2002. PMID: 12111112
-
Keratinocyte growth factor ameliorates radiation- and bleomycin-induced lung injury and mortality.Am J Pathol. 1996 Dec;149(6):1963-70. Am J Pathol. 1996. PMID: 8952531 Free PMC article.
-
Keratinocyte growth factor/fibroblast growth factor 7, a homeostatic factor with therapeutic potential for epithelial protection and repair.Adv Cancer Res. 2004;91:69-136. doi: 10.1016/S0065-230X(04)91003-2. Adv Cancer Res. 2004. PMID: 15327889 Review.
-
The effects of keratinocyte growth factor in preclinical models of mucositis.Cell Prolif. 2002 Aug;35 Suppl 1(Suppl 1):78-85. doi: 10.1046/j.1365-2184.35.s1.8.x. Cell Prolif. 2002. PMID: 12139710 Free PMC article. Review.
Cited by
-
An engineered biopolymer prevents mucositis induced by 5-fluorouracil in hamsters.Am J Pathol. 2004 Feb;164(2):739-46. doi: 10.1016/S0002-9440(10)63161-6. Am J Pathol. 2004. PMID: 14742277 Free PMC article.
-
Chimonanthus nitens var. salicifolius Aqueous Extract Protects against 5-Fluorouracil Induced Gastrointestinal Mucositis in a Mouse Model.Evid Based Complement Alternat Med. 2013;2013:789263. doi: 10.1155/2013/789263. Epub 2013 Dec 3. Evid Based Complement Alternat Med. 2013. PMID: 24367389 Free PMC article.
-
Gastro-intestinal toxicity of chemotherapeutics in colorectal cancer: the role of inflammation.World J Gastroenterol. 2014 Apr 14;20(14):3751-61. doi: 10.3748/wjg.v20.i14.3751. World J Gastroenterol. 2014. PMID: 24744571 Free PMC article. Review.
-
Modulation of specific intestinal epithelial progenitors by enteric neurons.Proc Natl Acad Sci U S A. 2001 Oct 23;98(22):12497-502. doi: 10.1073/pnas.211278098. Epub 2001 Sep 25. Proc Natl Acad Sci U S A. 2001. PMID: 11572941 Free PMC article.
-
Structural and functional alterations of the gastrointestinal tract following radiation-induced injury in the rhesus monkey.Dig Dis Sci. 2002 Jul;47(7):1480-91. doi: 10.1023/a:1015846514471. Dig Dis Sci. 2002. PMID: 12141804
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Molecular Biology Databases